ADHDgene Database

SNP Report

Basic Info

Name	rs2322333 dbSNP Ensembl
Location	Chr8:26695255(Fwd)
Variant Alleles	A/G
Ancestral Allele	G
Functional Annotation	NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant.
Consequence to Transcript	NMD_transcript_variant(ENST00000521711; ENST00000519096) intron_variant(ENST00000380582; ENST00000276393; ENST00000521711; ENST00000380573; ENST00000354550; ENST00000519096; ENST00000380586; ENST00000519229; ENST00000518621; ENST00000380572; ENST00000380587; ENST00000380581) nc_transcript_variant(ENST00000518621) upstream_gene_variant(ENST00000519826)
No. of Studies	1 (significant: 0; non-significant: 1; trend: 0)
Source	Literature-origin

SNP related studies (count: 1)

Reference	Allele Change	Risk Allele	Statistical Values	Author Comments	Result of Statistical Analysis
Hawi, Z., 2012	G:A	A	P-value=0.5571, X²=0.35, OR=1.08, 95% CI=0.83-1.3...... P-value=0.5571, X²=0.35, OR=1.08, 95% CI=0.83-1.39 More...	The marker did not show significant association with ADHD. The marker did not show significant association with ADHD.	Non-significant

SNP related genes (count: 2)

Approved Symbol	Approved Name	Location	No. of Studies (significant/non-significant/trend)
ADRA1A	adrenergic, alpha-1A-, receptor	8p21.2	3(2/1/0)

Approved Symbol	Approved Name	Location
COX6B1P4	cytochrome c oxidase subunit VIb polypeptide 1 (ubiquitous) pseudogene 4	8p21.2

SNPs in LD with rs2322333 (count: 2) View in gBrowse (chr8:26695255..26712981 )

The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r²>=0.8.

rs_ID	Functional Annotation	#studies(significant/non-significant/trend)	r²[population]

rs10503800	NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant	1(1/0/0)	0.866[CHD]; 0.95[JPT]